US20060280714A1 - Aluminum starch octenylsuccinate derivative of small-granule wheat starch and cosmetic formulations made therefrom - Google Patents

Aluminum starch octenylsuccinate derivative of small-granule wheat starch and cosmetic formulations made therefrom Download PDF

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US20060280714A1
US20060280714A1 US11/387,419 US38741906A US2006280714A1 US 20060280714 A1 US20060280714 A1 US 20060280714A1 US 38741906 A US38741906 A US 38741906A US 2006280714 A1 US2006280714 A1 US 2006280714A1
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aso
personal care
starch
care product
small
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US11/387,419
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Clodualdo Maningat
Sukh Bassi
Kyungsoo Woo
Dharmen Makwana
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MGP Ingredients Inc
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Assigned to MGP INGREDIENTS, INC. reassignment MGP INGREDIENTS, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: MAKWANA, DHARMEN B., MANINGAT, CLODUALDO C., WOO, KYUNGSOO, BASSI, SUKH D.
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/732Starch; Amylose; Amylopectin; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0241Containing particulates characterized by their shape and/or structure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B31/00Preparation of derivatives of starch
    • C08B31/02Esters
    • C08B31/04Esters of organic acids, e.g. alkenyl-succinated starch
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/41Particular ingredients further characterized by their size
    • A61K2800/412Microsized, i.e. having sizes between 0.1 and 100 microns
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/60Particulates further characterized by their structure or composition
    • A61K2800/65Characterized by the composition of the particulate/core
    • A61K2800/654The particulate/core comprising macromolecular material
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • A61Q1/04Preparations containing skin colorants, e.g. pigments for lips
    • A61Q1/06Lipsticks
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners

Definitions

  • the present invention generally pertains to an aluminum starch octenylsuccinate derivative of small-granule wheat starch, and cosmetic formulations including the aluminum starch octenylsuccinate derivative of small-granule wheat starch.
  • Starch is the predominant carbohydrate component of most cereals, legumes, tubers and root crops. It is deposited in plants as tiny, partially crystalline granules. The sizes, shapes, amylose contents and gelatinization temperatures of starch granules are affected by the botanical source of starch.
  • wheat two distinct classes of granules differing in size and shape have been reported by Seib, P.S. Wheat Starch: Isolation, Structure, and Properties. Oyo Toshitsu Kagaku 41: 49-69 (1994) and Cornell, H.J. and Hoveling, A.W. Wheat Chemistry and Utilization. Technomic Publishing, Lancaster, Pa. (1998).
  • the two classes are small ( ⁇ 5 ⁇ m), spherical granules and large ( ⁇ 20 ⁇ m), disk-shaped granules.
  • ASO aluminum starch octenylsuccinate
  • ASO is the aluminum salt of the reaction product of 1-octenylsuccinic anhydride with starch; see, e.g., U.S. Pat. Nos. 2,613,206 and 2,661,349.
  • ASO is not an ocular irritant and does not produce abnormal skin reactions in guinea pigs and rabbits (Anonymous “Final report on the safety assessment of aluminum starch octenyl succinate”, Int. J. Toxicol. 21: 1-7. (2003)).
  • ASO is used in cosmetic products up to 30% as an anti-caking agent and as a nonaqueous thickening agent.
  • ASO has been reported to enhance the sun protection factor of sunscreen formulations. For example, the sun protection factor value of titanium dioxide in a formulation can be enhanced by as much as 40% upon addition of as little as 5% aluminum starch octenylsuccinate.
  • wheat starches contain both small ( ⁇ 5 ⁇ m), spherical granules and large ( ⁇ 20 ⁇ m), disk-shaped granules.
  • the non-uniform size and morphology within the granular mixture can impact the properties and performance of the final product. For example, products made from wheat starch having a normal distribution of size and shape may not spread easily, may not provide a smooth finish and/or may not effectively absorb oil.
  • the present instrumentalities advance the art and overcome the problems that are outlined above.
  • aluminum starch octenylsuccinate has a distribution of starch granules with a mean diameter of between 4.5 ⁇ m and 8.9 ⁇ m.
  • the personal care products including the small-granule ASO may be selected from the group consisting of conditioning shampoo, damaged hair shampoo, hand cream, sunscreen lotion, liquid talc, a soap bar, lipstick, liquid make-up, and a mud mask.
  • a small-granule starch composition includes a plurality of starch granules having a size distribution with a mean diameter between 4.5 ⁇ m and 8.9 ⁇ m, the starch granules modified by reaction with 1-octenylsuccinic anhydride and an aluminum salt.
  • FIG. 1 shows a scanning electron micrograph (SEM) (1000x) of unmodified small-granule wheat starch.
  • FIG. 2 shows a scanning electron micrograph (SEM) (1000x) of unmodified normal-granule wheat starch.
  • FIG. 3 shows a scanning electron micrograph (SEM) (1000x) of small-granule aluminum starch octenylsuccinate.
  • FIG. 4 shows a scanning electron micrograph (SEM) (1000x) of normal-granule aluminum starch octenylsuccinate.
  • the present instrumentalities overcome the above described deficiencies and provide an aluminum starch octenylsuccinate derivative from wheat with a small average particle size.
  • the small-granule ASO derivative has a smooth feel, good slip, and high oil absorption capacity.
  • cosmetic products may be formulated to contain from 0.1-15% small-granule ASO wheat starch.
  • FIGS. 1 and 2 A comparison of the appearance of small-granule and normal-granule wheat starch is shown in FIGS. 1 and 2 , respectively. A predominance of small, spherical granules is evident in FIG. 1 , whereas both the large, disk-shaped and small, spherical granules appear in FIG. 2 .
  • the aluminum starch octenylsuccinate derivative brand name Skin Flow Ultra
  • modification of normal-granule wheat starch to yield the aluminum starch octenylsuccinate derivative shows the typical size and shape shown in FIG. 4 .
  • Oil absorption capacity was determined by following the procedure in ASTM D 281-95.
  • the oil absorption capacity of the aluminum starch octenylsuccinate derivative of small-granule wheat starch is 0.45 gram oil per gram of the small-granule wheat ASO versus 0.41 gram oil per gram of the normal-granule wheat ASO.
  • Water repellency was evaluated by adding 5 grams of starch sample to 75 ml of water in a graduated flask, gently mixing by inverting the flask ten times, and allowing the mixture to sit undisturbed for 1 hour. The mixture was mixed a second time by inverting the flask ten times and then allowed to sit undisturbed for 15 minutes. Water repellency after 15 minutes was determined by measuring the volume of sedimented starch in the flask. The water repellency of the ASO derivative of small-granule wheat starch was ⁇ 0.1 ml, whereas the water repellency of normal-granule wheat ASO was 7 ml. When applied to the skin, the ASO derivative of small-granule wheat starch appears to have a smoother, more velvety feel than the ASO derivative of normal-granule wheat starch.
  • a suitable primary tank In a suitable primary tank, the required amount of distilled water was metered out. Part A ingredients were added to the primary tank in the order listed. The Part B ingredients were then added to the primary tank. The Part C ingredients were added to the primary tank in the order listed. The pH was adjusted to 5.5-6.5 (25% AMP 95) and the viscosity was adjusted with NaCI to the desired thickness.
  • a suitable primary tank In a suitable primary tank, the required amount of distilled water was metered out. Part A ingredients were added to the primary tank in the order listed. The Part B ingredients were added to the primary tank. The Part C ingredients were added to the primary tank in the order listed. The pH was adjusted to 5.5-6.5 (25% AMP 95) and the viscosity was adjusted with NaCI to the desired thickness.
  • Part A ingredients were added to a primary tank and heated to 75° C.
  • Part B ingredients were heated to 75° C.
  • Part B was added to Part A.
  • the Part C ingredients were added to the batch at 65° C.
  • the Part D ingredients were added to the batch when the temperature reached 35° C.
  • Part A ingredients were added to the primary tank and heated to 75° C.
  • Part B ingredients were weighed out in the order listed and heated to 75° C.
  • Part B was added to Part A.
  • Part C was premixed and added to the batch at 70° C.
  • the Part D ingredients were added to the batch when the temperature reached 40° C.
  • Part A ingredients were added to a primary tank and heated to 75° C.
  • Part B ingredients were mixed and heated to 75° C.
  • Part B was added to Part A.
  • Part C was premixed and added to the batch at 55° C.
  • the Part D ingredients were added to the batch in the order listed when the temperature reached 35° C.
  • Part A In a suitable primary tank, the Part A ingredients were mixed and heated to 45° C. In a secondary tank, the Part B ingredients were premixed and combined with Part A. The mixture was stirred until tracing was observed ( ⁇ 20-25 minutes). Part C was added to the batch and stirred. Part D was added to the batch and stirred. The soap was poured into molds and then covered with a warm blanket for 24 hours. The soap was removed from the molds and allowed to cure for a few days.
  • Part A ingredients were added to a tank and heated to 75° C. In a secondary tank, the Part B ingredients were heated to 75° C. Part B was added to Part A. Part C and Part D were premixed and then added to the A-B mixture at 75° C. The temperature was maintained at 75° C until the color was uniform. The preservative and fragrance were added and then the mixture was set in molds at 45° C.
  • Part A ingredients were added to a tank and the mixture was heated to 75° C.
  • Part E ingredients were pressed through a colloid mill with some propylene glycol and recirculated until the pigments were evenly dispersed.
  • the colloid mill was rinsed with Part C and a lightning mixer was used to thoroughly mix the ingredients, which were heated to 75° C.
  • the Part B ingredients were premixed and heated to 75° C.
  • Part B was added to the main batch.
  • Part E was added to the main batch.
  • Part D was premixed and then added to the main batch when the temperature reached 65° C.
  • Part F was added to the main batch when the temperature reached 40° C.
  • the preservative and fragrance were added. The pH and viscosity were adjusted to desired levels.
  • Part A ingredients were added to a tank and mixed until a uniform solution resulted. The solution was then heated to 75° C. and cooling was started. When the temperature reached 45° C., the Part C ingredients were sprinkled into Part A in the order listed. Part B was added to the batch. The ingredients of Part D were premixed and added to the batch.

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Abstract

A small-granule aluminum starch octenylsuccinate (ASO) derivative having a distribution of starch granules with a mean diameter of between 4.5 μm and 8.9 μm is disclosed herein. The small-granule ASO may be used in a wide variety of personal care formulations.

Description

    RELATED APPLICATIONS
  • This application claims the benefit of priority to U.S. provisional patent application Ser. No. 60/664,433, filed Mar. 23, 2005 and U.S. provisional patent application Ser. No. 60/664,814, filed Mar. 24, 2005, each of which is incorporated herein by reference.
  • FIELD OF THE INVENTION
  • The present invention generally pertains to an aluminum starch octenylsuccinate derivative of small-granule wheat starch, and cosmetic formulations including the aluminum starch octenylsuccinate derivative of small-granule wheat starch.
  • BACKGROUND
  • Starch is the predominant carbohydrate component of most cereals, legumes, tubers and root crops. It is deposited in plants as tiny, partially crystalline granules. The sizes, shapes, amylose contents and gelatinization temperatures of starch granules are affected by the botanical source of starch. In wheat, two distinct classes of granules differing in size and shape have been reported by Seib, P.S. Wheat Starch: Isolation, Structure, and Properties. Oyo Toshitsu Kagaku 41: 49-69 (1994) and Cornell, H.J. and Hoveling, A.W. Wheat Chemistry and Utilization. Technomic Publishing, Lancaster, Pa. (1998). The two classes are small (˜5 μm), spherical granules and large (˜20 μm), disk-shaped granules.
  • Personal care products usually contain starch in the form of aluminum starch octenylsuccinate (ASO), which is the aluminum salt of the reaction product of 1-octenylsuccinic anhydride with starch; see, e.g., U.S. Pat. Nos. 2,613,206 and 2,661,349. ASO is not an ocular irritant and does not produce abnormal skin reactions in guinea pigs and rabbits (Anonymous “Final report on the safety assessment of aluminum starch octenyl succinate”, Int. J. Toxicol. 21: 1-7. (2003)). It is nontoxic to rats by inhalation, and clinical facial sting, chamber scarification, and closed patched studies indicated little irritation potential when ASO was tested up to 3% in cosmetic formulations. ASO is used in cosmetic products up to 30% as an anti-caking agent and as a nonaqueous thickening agent. Guth et al. “Polymeric approaches to skin protection”, Cosmet. Toiletries 106: 71-74 (1991) described the performance of aluminum starch octenylsuccinate as an aesthetics control agent in creams and lotions, where it may be used to mitigate the greasiness and drag often associated with products containing high levels of occlusive agents or organic-based UV absorbers. ASO has been reported to enhance the sun protection factor of sunscreen formulations. For example, the sun protection factor value of titanium dioxide in a formulation can be enhanced by as much as 40% upon addition of as little as 5% aluminum starch octenylsuccinate.
  • Commercially-available wheat starches contain both small (˜5 μm), spherical granules and large (˜20 μm), disk-shaped granules. When wheat starch is used in personal care products, the non-uniform size and morphology within the granular mixture can impact the properties and performance of the final product. For example, products made from wheat starch having a normal distribution of size and shape may not spread easily, may not provide a smooth finish and/or may not effectively absorb oil.
  • SUMMARY
  • The present instrumentalities advance the art and overcome the problems that are outlined above.
  • In one aspect, aluminum starch octenylsuccinate (ASO) has a distribution of starch granules with a mean diameter of between 4.5 μm and 8.9 μm. The personal care products including the small-granule ASO may be selected from the group consisting of conditioning shampoo, damaged hair shampoo, hand cream, sunscreen lotion, liquid talc, a soap bar, lipstick, liquid make-up, and a mud mask.
  • In one aspect a small-granule starch composition includes a plurality of starch granules having a size distribution with a mean diameter between 4.5 μm and 8.9 μm, the starch granules modified by reaction with 1-octenylsuccinic anhydride and an aluminum salt.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 shows a scanning electron micrograph (SEM) (1000x) of unmodified small-granule wheat starch.
  • FIG. 2 shows a scanning electron micrograph (SEM) (1000x) of unmodified normal-granule wheat starch.
  • FIG. 3 shows a scanning electron micrograph (SEM) (1000x) of small-granule aluminum starch octenylsuccinate.
  • FIG. 4 shows a scanning electron micrograph (SEM) (1000x) of normal-granule aluminum starch octenylsuccinate.
  • DETAILED DESCRIPTION
  • The present instrumentalities overcome the above described deficiencies and provide an aluminum starch octenylsuccinate derivative from wheat with a small average particle size. The small-granule ASO derivative has a smooth feel, good slip, and high oil absorption capacity. In one embodiment, cosmetic products may be formulated to contain from 0.1-15% small-granule ASO wheat starch.
  • The following examples set forth the preparation of the aluminum starch octenylsuccinate derivative of small-granule wheat starch and the formulation of this starch derivative in several cosmetic products. It is to be understood, however, that these examples are provided by way of illustration, and not by limitation, to illustrate preferred embodiments of what is claimed.
  • EXAMPLE 1 Preparation and Characterization of Aluminum Starch Octenylsuccinate Derivative of Small-Granule Wheat Starch
  • Starch Modification. Commercially available small-granule wheat starch (brand name Puramyl SP) was purchased from Latenstein BV (Netherlands). The starch was dispersed in water and modified with 1-octenylsuccinic anhydride and aluminum sulfate according to the provisions of the U.S. Code of Federal Regulations (Title 21 CFR §172.892) for Food Starch-Modified.
  • Starch Characterization. Granule size distribution was determined using a Coulter MultiSizer II (Beckman Coulter, Inc., Miami, Fla.). Using number statistics, the small-granule wheat starch (Puramyl SP) shows a mean diameter of 4.5 μm. By volume statistics, the mean diameter is 8.9 μm. In contrast, normal wheat starch (brand name Midsol 50 from MGP Ingredients, Inc., Atchison, Kans.) has a mean diameter of 10.6 and 18.1 μm by number statistics and volume statistics, respectively.
    TABLE 1
    Mean diameter of small-granule wheat starch and normal-granule
    wheat starch.
    Mean Diameter by Mean Diameter by
    Starch Samples Number Statistics Volume Statistics
    Small-Granule  4.5 μm  8.9 μm
    Wheat Starch
    Normal-Granule 10.6 μm 18.1 μm
    Wheat Starch
  • Surface topography of starch granules was determined using a scanning electron microscope. Samples were gold coated with a Hummer Sputter Coating System and imaged with a Hitachi 3000N Scanning Electron Microscope. A comparison of the appearance of small-granule and normal-granule wheat starch is shown in FIGS. 1 and 2, respectively. A predominance of small, spherical granules is evident in FIG. 1, whereas both the large, disk-shaped and small, spherical granules appear in FIG. 2. After modification of small-granule wheat starch, the aluminum starch octenylsuccinate derivative (brand name Skin Flow Ultra) exhibits the typical size and shape shown in FIG. 3. Similarly, modification of normal-granule wheat starch to yield the aluminum starch octenylsuccinate derivative (brand name Skin Flow) shows the typical size and shape shown in FIG. 4. Oil absorption capacity was determined by following the procedure in ASTM D 281-95. The oil absorption capacity of the aluminum starch octenylsuccinate derivative of small-granule wheat starch is 0.45 gram oil per gram of the small-granule wheat ASO versus 0.41 gram oil per gram of the normal-granule wheat ASO. Water repellency was evaluated by adding 5 grams of starch sample to 75 ml of water in a graduated flask, gently mixing by inverting the flask ten times, and allowing the mixture to sit undisturbed for 1 hour. The mixture was mixed a second time by inverting the flask ten times and then allowed to sit undisturbed for 15 minutes. Water repellency after 15 minutes was determined by measuring the volume of sedimented starch in the flask. The water repellency of the ASO derivative of small-granule wheat starch was <0.1 ml, whereas the water repellency of normal-granule wheat ASO was 7 ml. When applied to the skin, the ASO derivative of small-granule wheat starch appears to have a smoother, more velvety feel than the ASO derivative of normal-granule wheat starch.
  • EXAMPLE 2
  • PREPARATION OF CONDITIONING SHAMPOO
    Trade Name INCI Name W/W %
    A Water Aqua Adjust
    A ETD 2020 Acrylate/C10-30 Alkyl 0.20
    Acrylate Crosspolymer
    A PK-771 PVP 2.80
    A Merquat 550 Polyquaternium-7 0.10
    A Versene NA2 Disodium EDTA 0.10
    A Jeechem GC-7 PEG-7 Glycerox HE 0.20
    A Stepanol CS-230 Sodium Laureth Sulfate 25.00
    A Stepanol WAC Sodium Lauryl Sulfate 10.00
    A Mackham 35 Cocomidopropyl Betaine 2.50
    A Jojoba Oil Yellow Simmondsia Chinensis 0.50
    A Almond Oil Prunus Amygdalus Dulcis 0.10
    A Skin Flow Ultra Aluminum Starch 0.50
    Octenylsuccinate
    A Glycerin USP Glycerol 2.00
    B D-L Panthenol Panthenol 0.05
    B Aloe Vera Extract Aloe Barbadensis 0.03
    B Rosehip Extract Rosa Canina 0.06
    C Preservative Propylene Glycol and 0.40
    Diazolidinyl Urea and
    Methylparaben and
    Propylparaben
    C Fragrance Fragrance 0.10
    C Blue # 1 FD&C Blue # 01 QS

    QS = quality standard
  • In a suitable primary tank, the required amount of distilled water was metered out. Part A ingredients were added to the primary tank in the order listed. The Part B ingredients were then added to the primary tank. The Part C ingredients were added to the primary tank in the order listed. The pH was adjusted to 5.5-6.5 (25% AMP 95) and the viscosity was adjusted with NaCI to the desired thickness.
  • EXAMPLE 3
  • PREPARATION OF DAMAGED HAIR SHAMPOO
    Trade Name INCI Name W/W %
    A Water Aqua Adjust
    A ETD 2020 Acrylate/C10-30 Alkyl 0.20
    Acrylate Crosspolymer
    A PK-771 PVP 2.80
    A Jeechem GC-7 PEG-7 Glycerox HE 0.20
    A Glycerin Glycerol 1.00
    A Jeelate ES-2 Sodium Laureth Sulfate 25.00
    A Stepanol WAC Sodium Lauryl Sulfate 10.00
    A Mackham 35 Cocomidopropyl Betaine 2.50
    A Jojoba Oil Yellow Simmondsia Chinensis 0.50
    A Almond Oil Prunus Amygdalus Dulcis 0.10
    A Skin Flow Ultra Aluminum Starch 0.50
    Octenylsuccinate
    B D-L Panthenol Panthenol 0.05
    C Preservative Propylene Glycol and 0.40
    Diazolidinyl Urea and
    Methylparaben and
    Propylparaben
    C Aqua Pro ® II WP Hydrolyzed Wheat Protein 1.50
    C Fragrance Fragrance 0.10
    C Blue # 1 FD&C Blue # 01 QS

    QS = quality standard
  • In a suitable primary tank, the required amount of distilled water was metered out. Part A ingredients were added to the primary tank in the order listed. The Part B ingredients were added to the primary tank. The Part C ingredients were added to the primary tank in the order listed. The pH was adjusted to 5.5-6.5 (25% AMP 95) and the viscosity was adjusted with NaCI to the desired thickness.
  • EXAMPLE 4
  • PREPARATION OF HAND CREAM
    Trade Name INCI Name W/W %
    A Water Aqua QS
    A Glycerin Glycerin 1.50
    A Skin Flow Ultra Aluminum Starch 2.00
    Octenylsuccinate
    B Jeen Stearic Acid Stearic Acid 3.00
    B Lipo GMS 450 Glyceryl Sterate 2.00
    B Lipocol C Cetyl Alcohol 2.00
    B Promulgin D Cetearyl Alcohol and 1.00
    Ceteareth-20
    B Lipocol S Steraryl Alcohol 1.00
    B Coconut Oil Theobromo Cacao 0.50
    B Lipo IPM Isopropyl Myristate 0.50
    B Lipo IPP Isopropyl Palmitate 0.50
    B Jojoba Oil Simmondsia Chinensis 0.75
    B Nipagin M Methylparaben 0.20
    B Nipasol M Propylparaben 0.15
    C Dow Corning 200 Dimethicone 0.50
    Fluid
    C Phenoxyethanol Phenoxyethanol 0.30
    D Fragrance Fragrance QS
  • Part A ingredients were added to a primary tank and heated to 75° C. In a secondary tank, the Part B ingredients were heated to 75° C. Part B was added to Part A. With good mixing, the Part C ingredients were added to the batch at 65° C. The Part D ingredients were added to the batch when the temperature reached 35° C.
  • EXAMPLE 5
  • PREPARATION OF SUNSCREEN MOISTURIZING LOTION
    Trade Name INCI Name W/W %
    A Water Aqua Adjust
    A Versene NA Disodium EDTA 0.10
    A Acritamer 940 Carbomer 0.15
    A AMP 95 Regular 2-Amino-2-Methyl-1-Propanol QS
    B Jeen Stearic Acid Stearic Acid 2.00
    B Promulgin D Cetearyl Alcohol and 1.50
    Ceteareth-20
    B Liponate SPS Cetyl Ester 1.50
    B Lipovol MS-70 Mineral Oil 0.50
    B Lipo GMS 450 Glyceryl Sterate 2.50
    B Dow Corning 200-350 ct Dimethicone 0.50
    B Jeescreen OMC Ethylhexyl Methoxycinnamate 7.00
    C Finsol TN C12-15 Alkyl Benzoate 2.75
    C Skin Flow Ultra Aluminum Starch 2.00
    Octenylsuccinate
    D Liquapar PE Phenoxyethanol (and) QS
    Isopropylparaben (and)
    Isobutylparaben (and)
    Butylparaben
    D Fragrance Fragrance 0.05
  • In a suitable primary tank, the required amount of distilled water was metered out. Part A ingredients were added to the primary tank and heated to 75° C. In a secondary tank, the Part B ingredients were weighed out in the order listed and heated to 75° C. Part B was added to Part A. Part C was premixed and added to the batch at 70° C. The Part D ingredients were added to the batch when the temperature reached 40° C.
  • EXAMPLE 6
  • PREPARATION OF REFRESHING LIQUID TALC (LOTION)
    Trade Name INCI Name W/W %
    A Water Aqua 67.4
    A Glycerin USP Glycerin 1.00
    B Lipocol C Cetyl Alcohol 1.50
    B Jeen Stearic Acid Stearic Acid 1.50
    B Lopocol S Stearyl Alcohol 0.50
    B Promulgin D Cetearyl Alcohol and 0.80
    Ceteareth-20
    B Rita GMS Glyceryl Sterate 0.50
    B Kessco IPP Isopropylpalmitate 1.00
    B Dow Corning-200 Dimethicone 0.20
    C Skin Flow Ultra Aluminum Starch 3.00
    Octenylsuccinate
    C Lipo IPM Isopropyl Myristate 2.00
    D SD-40 Alcohol 20.0
    D Fragrance Fragrance 0.20
    (Plumeria)
    D Liquapar PE Phenoxyethanol (and) 0.40
    Isopropylparaben (and)
    Isobutylparaben (and)
    Butylparaben

    QS = Quality Standard
  • The Part A ingredients were added to a primary tank and heated to 75° C. In a secondary tank, the Part B ingredients were mixed and heated to 75° C. Part B was added to Part A. Part C was premixed and added to the batch at 55° C. The Part D ingredients were added to the batch in the order listed when the temperature reached 35° C.
  • EXAMPLE 7
  • PREPARATION OF MOISTURIZING SOAP BAR
    Trade Name INCI Name Grams
    A Almond Oil Pruns Amygdalus Dulcis 2.00
    A Canola Oil Canola Oil 10.00
    A Coconut Oil Theobromo Cacao 20.00
    A Jojoba Oil Simmondsia Chinensis 3.00
    A Mango Oil Mangifera Indica 3.00
    A Palm Kernel Oil Elaeis Guineensis Oil 10.00
    A Safflower Oil Carthamus Tinctorius 12.00
    A Soybean Oil Glycine Soja Oil 7.00
    A Sunflower Oil Helianthus Annuus Oil 4.00
    B Sodium Hydroxide1 Sodium Hydroxide 20.00
    B Water Aqua 19.00
    B Skin Flow Ultra Aluminum Starch 5.00
    Octenylsuccinate
    C Foam Pro L Hydrolyzed Wheat Protein 4.00
    D Fragrance Fragrance 3.00
    D Color Color QS

    QS = quality standard

    1Sodium Hydroxide 50%
  • In a suitable primary tank, the Part A ingredients were mixed and heated to 45° C. In a secondary tank, the Part B ingredients were premixed and combined with Part A. The mixture was stirred until tracing was observed (˜20-25 minutes). Part C was added to the batch and stirred. Part D was added to the batch and stirred. The soap was poured into molds and then covered with a warm blanket for 24 hours. The soap was removed from the molds and allowed to cure for a few days.
  • EXAMPLE 8
  • PREPARATION OF MOISTURIZING LIPSTICK
    Trade Name INCI Name W/W %
    A Castor Oil Ricinus Communis Adjust
    A Candelilla Wax Euphorbia Cerfera 4.50
    A Carnauba Wax Copernicia Cerfera 1.50
    A Ozokerite Wax Ozokerite 1.25
    A Microcrystalline Microcrystalline Wax 2.50
    Wax
    B Liponate CG Caprylic Capric Triglyceride 12.00 
    B Lipovol MOS-70 Mineral Oil 1.50
    B Jeechem OOS Octyldodecyl Stearoyl Sterate 4.00
    B Lipo IPM Isopropyl Myristate 1.00
    B Lipo IPP Isopropyl Palmitate 1.00
    B Tocopheryl Acetate Tocopheryl Acetate 0.05
    C Yellow Iron Oxide Iron Oxide Yellow QS
    C Black Iron Oxide Iron Oxide Black QS
    C Red Iron Oxide Iron Oxide Red QS
    D Castor Oil Ricinus Communis 5.00
    D Skin Flow Ultra Aluminum Starch 2.00
    Octenylsuccinate
    E Nipagin M Methylparaben 0.20
    E Nipasol M Propylparaben 0.15
    E Fragrance Fragrance QS
  • Part A ingredients were added to a tank and heated to 75° C. In a secondary tank, the Part B ingredients were heated to 75° C. Part B was added to Part A. Part C and Part D were premixed and then added to the A-B mixture at 75° C. The temperature was maintained at 75° C until the color was uniform. The preservative and fragrance were added and then the mixture was set in molds at 45° C.
  • EXAMPLE 9
  • PREPARATION OF LIQUID MAKE-UP
    Trade Name INCI Name W/W %
    A Deionized Water Aqua Adjust
    A Triethanolamine Triethanolamine QS
    (99%)
    A Propylene Glycol 5.00
    (Universal)
    A Carbomer 940 Carbomer 0.20
    A Veegum 0.30
    A Skin Flow Ultra Aluminum Starch 2.00
    Octenylsuccinate
    B Stearic Acid (Lipo) 1.00
    B PEG-120 Dimethyl 1.00
    Glucose
    Sesquesterate
    B Stearate-20 0.80
    B Cetyl Alcohol 0.50
    B Ceteth-20 0.50
    B Methyl Glucose 1.00
    Sesquesterate
    B Nylon-12 (Lipo) 3.50
    C Isopar-G 0.20
    C Isopar-M 0.20
    D Silica Dimethyl 1.00
    Siliylate (Cabot)
    D Cyclomethicone 15.00
    (Dow Corning)
    E Titanium Dioxide 2.00
    (Rona)
    E Iron Oxide Yellow 0.40
    (BF Goodrich)
    E Iron Oxide Black 0.20
    (BF Goodrich)
    E Iron Oxide Red (BF 0.30
    Goodrich)
    F Polysorbate-20 1.00
    G Preservative QS
    H Fragrance QS
  • Part A ingredients were added to a tank and the mixture was heated to 75° C. Part E ingredients were pressed through a colloid mill with some propylene glycol and recirculated until the pigments were evenly dispersed. The colloid mill was rinsed with Part C and a lightning mixer was used to thoroughly mix the ingredients, which were heated to 75° C. In a secondary tank, the Part B ingredients were premixed and heated to 75° C. Part B was added to the main batch. Part E was added to the main batch. Part D was premixed and then added to the main batch when the temperature reached 65° C. Part F was added to the main batch when the temperature reached 40° C. The preservative and fragrance were added. The pH and viscosity were adjusted to desired levels.
  • EXAMPLE 10
  • PREPARATION OF REFRESHING MUD MASK
    Trade Name INCI Name W/W %
    A Water Aqua Adjust
    A Carbomer 940 Carbomer 0.15
    A Triethanolamine Triethanolamine QS
    (99%)
    A Skin Flow Ultra Aluminum Starch 1.00
    Octenylsuccinate
    B Propylene Glycol Propylene Glycol 5.00
    B L-Menthol L-Menthol 0.10
    C China Clay Clay 12.00 
    C Eusolex T-200 Titanium Dioxide 0.50
    D Preservative Preservative QS
    D Aqua Pro ® WP Hydrolyzed Wheat Protein 1.50
    D Aqua Pro ® WAA Wheat Amino Acid 0.50
    D Fennel Extract Fennel Extract 0.50
  • Part A ingredients were added to a tank and mixed until a uniform solution resulted. The solution was then heated to 75° C. and cooling was started. When the temperature reached 45° C., the Part C ingredients were sprinkled into Part A in the order listed. Part B was added to the batch. The ingredients of Part D were premixed and added to the batch.
  • Changes may be made in the above compositions and methods without departing from the subject matter described in the Summary and defined by the following claims. It should thus be noted that the matter contained in the above description should be interpreted as illustrative and not limiting.
  • All references cited are incorporated by reference herein.

Claims (20)

1. Aluminum starch octenylsuccinate (ASO) having a number mean diameter of about 4.5 μm.
2. The ASO of claim 1 further comprising a water repellency less than about 0.1 ml of sedimented starch per 5 grams of sample dispersed in 75 ml water.
3. The ASO of claim 1 further comprising a oil absorption capacity in excess of about 0.45 grams of oil per gram of sample.
4. A personal care product including the ASO of claim 1.
5. A personal care product comprising from 0.1 -10% by weight of the ASO of claim 1.
6. The personal care product of claim 4, wherein the personal care product is selected from the group consisting of conditioning shampoo, damaged hair shampoo, hand cream, sunscreen lotion, liquid talc, a soap bar, lipstick, liquid make-up, and a mud mask.
7. A personal care product comprising from 0.5-10% by weight of the ASO of claim 1.
8. A small-granule starch composition comprising:
a plurality of starch granules having a number mean diameter of about 4.5 μm, said starch granules modified by reaction with 1-octenylsuccinic anhydride and an aluminum salt.
9. A personal care product including the composition of claim 8.
10. A personal care product comprising from 0.1-10% by weight of the composition of claim 8.
11. The personal care product of claim 9, wherein the personal care product is selected from the group consisting of conditioning shampoo, damaged hair shampoo, hand cream, sunscreen lotion, liquid talc, a soap bar, lipstick, liquid make-up, and a mud mask.
12. A personal care product comprising from 0.5-10% by weight of the composition of claim 8.
13. The composition of claim 8, wherein said starch granules further comprise a volume mean diameter of about 8.9 μm.
14. A composition comprising aluminum starch octenylsuccinate (ASO) having a volume mean diameter of about 8.9 μm.
15. The ASO of claim 14 further comprising a water repellency less than about 0.1 ml of sedimented starch per 5 grams of sample dispersed in 75 ml water.
16. The ASO of claim 14 further comprising a oil absorption capacity in excess of about 0.45 grams of oil per gram of sample.
17. A personal care product including the ASO of claim 14.
18. The personal care product of claim 17, wherein the personal care product is selected from the group consisting of conditioning shampoo, damaged hair shampoo, hand cream, sunscreen lotion, liquid talc, a soap bar, lipstick, liquid make-up, and a mud mask.
19. A personal care product comprising from 0.1-10% by weight of the ASO of claim 14.
20. A personal care product comprising from 0.5-10% by weight of the ASO of claim 14.
US11/387,419 2005-03-23 2006-03-23 Aluminum starch octenylsuccinate derivative of small-granule wheat starch and cosmetic formulations made therefrom Abandoned US20060280714A1 (en)

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US20070025941A1 (en) * 2005-08-01 2007-02-01 L'oréal Liquid lip gloss compositions with enhanced shine
FR2925300A1 (en) * 2007-12-21 2009-06-26 Oreal COSMETIC MAKE-UP AND / OR CARE COMPOSITION COMPRISING AN ASSOCIATION OF TWO PARTICULAR CHARGES AND A HIGH VISCOSITY FAT BODY
US20110082290A1 (en) * 2009-10-07 2011-04-07 Akzo Nobel Chemicals International B.V. Superhydrophilic amphiphilic copolymers and processes for making the same
US20110081309A1 (en) * 2009-10-07 2011-04-07 Fevola Michael J Compositions comprising a superhydrophilic amphiphilic copolymer and a micellar thickener
EP2067466B1 (en) * 2007-12-03 2012-08-15 Varatus Vongsurakrai Cosmetic and/or dermatological powder comprising modified starch
US9114154B2 (en) 2009-10-07 2015-08-25 Johnson & Johnson Consumer Inc. Compositions comprising superhydrophilic amphiphilic copolymers and methods of use thereof
US20170007507A1 (en) * 2014-02-07 2017-01-12 Coty Inc. Free standing color cosmetic stick
EP2882498B1 (en) 2012-08-13 2017-08-30 Henkel AG & Co. KGaA Agent and method for the temporary deformation of keratin fibres
WO2017220254A1 (en) * 2016-06-21 2017-12-28 Unilever N.V. Skin care composition
US10603261B2 (en) 2014-12-19 2020-03-31 The Procter And Gamble Company Composition for enhancing hair fiber properties
US10722436B2 (en) * 2015-08-10 2020-07-28 Mary Kay Inc. Topical compositions
WO2020190697A1 (en) * 2019-03-19 2020-09-24 Cargill, Incorporated High oil content topical personal care products
US11129780B2 (en) 2016-01-29 2021-09-28 The Procter And Gamble Company Composition for enhancing hair fiber properties
US20230000754A1 (en) * 2020-12-08 2023-01-05 Jiangnan University Liquid Foundation Using Starch as Filler and Preparation Method thereof
US20230323251A1 (en) * 2020-09-09 2023-10-12 Conopco, lnc., d/b/a UNILEVER Laundry composition

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US20070025941A1 (en) * 2005-08-01 2007-02-01 L'oréal Liquid lip gloss compositions with enhanced shine
EP2067466B1 (en) * 2007-12-03 2012-08-15 Varatus Vongsurakrai Cosmetic and/or dermatological powder comprising modified starch
FR2925300A1 (en) * 2007-12-21 2009-06-26 Oreal COSMETIC MAKE-UP AND / OR CARE COMPOSITION COMPRISING AN ASSOCIATION OF TWO PARTICULAR CHARGES AND A HIGH VISCOSITY FAT BODY
WO2009080623A1 (en) * 2007-12-21 2009-07-02 L'oreal Cosmetic composition for make-up and/or care containing a combination of two particular fillers and a fatty substance of high viscosity
US20110081309A1 (en) * 2009-10-07 2011-04-07 Fevola Michael J Compositions comprising a superhydrophilic amphiphilic copolymer and a micellar thickener
US8399590B2 (en) * 2009-10-07 2013-03-19 Akzo Nobel Chemicals International B.V. Superhydrophilic amphiphilic copolymers and processes for making the same
US9114154B2 (en) 2009-10-07 2015-08-25 Johnson & Johnson Consumer Inc. Compositions comprising superhydrophilic amphiphilic copolymers and methods of use thereof
US9243074B2 (en) 2009-10-07 2016-01-26 Akzo Nobel Chemicals International B.V. Superhydrophilic amphiphilic copolymers and processes for making the same
US20110082290A1 (en) * 2009-10-07 2011-04-07 Akzo Nobel Chemicals International B.V. Superhydrophilic amphiphilic copolymers and processes for making the same
US11173106B2 (en) 2009-10-07 2021-11-16 Johnson & Johnson Consumer Inc. Compositions comprising a superhydrophilic amphiphilic copolymer and a micellar thickener
EP2882498B1 (en) 2012-08-13 2017-08-30 Henkel AG & Co. KGaA Agent and method for the temporary deformation of keratin fibres
US20170007507A1 (en) * 2014-02-07 2017-01-12 Coty Inc. Free standing color cosmetic stick
US10603261B2 (en) 2014-12-19 2020-03-31 The Procter And Gamble Company Composition for enhancing hair fiber properties
US11179305B2 (en) 2015-08-10 2021-11-23 Mary Kay Inc. Topical compositions
US10722436B2 (en) * 2015-08-10 2020-07-28 Mary Kay Inc. Topical compositions
US11129780B2 (en) 2016-01-29 2021-09-28 The Procter And Gamble Company Composition for enhancing hair fiber properties
US11986542B2 (en) 2016-01-29 2024-05-21 The Procter & Gamble Company Composition for enhancing hair fiber properties
CN109310593A (en) * 2016-06-21 2019-02-05 荷兰联合利华有限公司 Skin care compositions and methods
US10709652B2 (en) 2016-06-21 2020-07-14 Conopco, Inc. Skin care composition
WO2017220254A1 (en) * 2016-06-21 2017-12-28 Unilever N.V. Skin care composition
CN113645943A (en) * 2019-03-19 2021-11-12 嘉吉公司 Topical personal care products with high oil content
WO2020190697A1 (en) * 2019-03-19 2020-09-24 Cargill, Incorporated High oil content topical personal care products
US12251455B2 (en) 2019-03-19 2025-03-18 Cargill, Incorporated High oil content topical personal care products
US20230323251A1 (en) * 2020-09-09 2023-10-12 Conopco, lnc., d/b/a UNILEVER Laundry composition
US20230000754A1 (en) * 2020-12-08 2023-01-05 Jiangnan University Liquid Foundation Using Starch as Filler and Preparation Method thereof

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